Document Detail


CLOCK genetic variation and metabolic syndrome risk: modulation by monounsaturated fatty acids.
MedLine Citation:
PMID:  19846548     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Disruption of the circadian system may be causal for manifestations of the metabolic syndrome (MetS).
OBJECTIVE: The objective was to study the associations of 5 CLOCK polymorphisms with MetS features by analyzing fatty acid (FA) composition from dietary and red blood cell (RBC) membrane sources.
DESIGN: Participants (n = 1100) in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) study were included. Dietary intake was estimated with a validated questionnaire. Anthropometric and biochemical measurements and genotypes were determined. Postprandial lipids and the FA composition of RBC membranes were analyzed.
RESULTS: CLOCK single nucleotide polymorphisms were significantly associated with obesity and individual components of MetS. For single nucleotide polymorphism rs4580704, minor allele carriers had a 46% lower risk of hypertension than did noncarriers. The monounsaturated fatty acid (MUFA) content of RBC membranes, particularly oleic acid, changed according to CLOCK genetic variants (P < 0.05). We identified significant gene-diet interactions associated with MetS at the CLOCK locus. By dichotomizing MUFA intake, we found different effects across rs4580704 genotypes for glucose (P = 0.020) and insulin resistance (P = 0.026). The protective effect of the minor allele on insulin sensitivity was only present when MUFA intake was >13.2% of energy. We also found different effects across CLOCK 3111T-->C genotypes for saturated fatty acid intake (% of energy) (P = 0.017). The deleterious effect of gene variants on waist circumference was only found with high saturated fatty acid intakes (>11.8%).
CONCLUSIONS: CLOCK polymorphisms interact with FAs to modulate MetS traits. The dietary source and membrane content of MUFAs are implicated in the relations between alterations in the circadian system and MetS.
Authors:
Marta Garaulet; Yu-Chi Lee; Jian Shen; Laurence D Parnell; Donna K Arnett; Michael Y Tsai; Chao-Qiang Lai; Jose M Ordovas
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2009-10-21
Journal Detail:
Title:  The American journal of clinical nutrition     Volume:  90     ISSN:  1938-3207     ISO Abbreviation:  Am. J. Clin. Nutr.     Publication Date:  2009 Dec 
Date Detail:
Created Date:  2009-11-25     Completed Date:  2009-12-08     Revised Date:  2013-05-31    
Medline Journal Info:
Nlm Unique ID:  0376027     Medline TA:  Am J Clin Nutr     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1466-75     Citation Subset:  AIM; IM    
Affiliation:
Department of Physiology, University of Murcia, Murcia, Spain. garaulet@um.es
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MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Body Mass Index
CLOCK Proteins / genetics*
Erythrocyte Membrane / chemistry
Fatty Acids, Monounsaturated / administration & dosage*,  analysis
Female
Genotype
Haplotypes
Humans
Insulin Resistance
Male
Metabolic Syndrome X / etiology*,  genetics
Middle Aged
Polymorphism, Single Nucleotide*
Risk
Grant Support
ID/Acronym/Agency:
1R21AR055228-01A1/AR/NIAMS NIH HHS; DK075030/DK/NIDDK NIH HHS; HL54776/HL/NHLBI NIH HHS; U01 HL72524/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Fatty Acids, Monounsaturated; EC 2.3.1.48/CLOCK Proteins; EC 2.3.1.48/CLOCK protein, human
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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